Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.08 (G)

Chromosome 8:127416506 (forward strand) | View in location tab


with COSMIC COSM3982391 (A/G), COSM3982390 (A/G) ; HGMD-PUBLIC CM073273 ; dbSNP rs71520669 (A/G)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts and has 1095 individual genotypes.

Variation displays